@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_head
{
this:
np:hasAssertion
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_assertion
;
np:hasProvenance
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_assertion
a
np:Assertion
.
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_provenance
a
np:Provenance
.
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_assertion
{
miriam-gene:31
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN8cb96abee0f1fe77a6917c3cec36a862
sio:SIO_000628
miriam-gene:31
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_provenance
{
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_assertion
dcterms:description
"[These data suggested that the -1154/, 936/ and -2578/ ACC haplotype was associated with the risk of acute cerebral infarction with an OR of 0.361, and it may reduce the risk of acute cerebral infarction through the regulation of VEGF expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21757917
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP353133.RA2_kB86gUOL0Hpjbkg4IxhCiA5aHzu7NFQ2XtMvBEKcQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}